Department of Clinical Sciences, Section for Clinical and Experimental Infection Medicine, Lund University, Lund, Sweden.
PLoS Pathog. 2009 Dec;5(12):e1000698. doi: 10.1371/journal.ppat.1000698. Epub 2009 Dec 18.
Protein C inhibitor (PCI) is a heparin-binding serine proteinase inhibitor belonging to the family of serpin proteins. Here we describe that PCI exerts broad antimicrobial activity against bacterial pathogens. This ability is mediated by the interaction of PCI with lipid membranes, which subsequently leads to their permeabilization. As shown by negative staining electron microscopy, treatment of Escherichia coli or Streptococcus pyogenes bacteria with PCI triggers membrane disruption followed by the efflux of bacterial cytosolic contents and bacterial killing. The antimicrobial activity of PCI is located to the heparin-binding site of the protein and a peptide spanning this region was found to mimic the antimicrobial activity of PCI, without causing lysis or membrane destruction of eukaryotic cells. Finally, we show that platelets can assemble PCI on their surface upon activation. As platelets are recruited to the site of a bacterial infection, these results may explain our finding that PCI levels are increased in tissue biopsies from patients suffering from necrotizing fasciitis caused by S. pyogenes. Taken together, our data describe a new function for PCI in innate immunity.
蛋白 C 抑制剂 (PCI) 是一种肝素结合丝氨酸蛋白酶抑制剂,属于丝氨酸蛋白酶抑制剂家族。在这里,我们描述了 PCI 对细菌病原体具有广泛的抗菌活性。这种能力是通过 PCI 与脂质膜的相互作用介导的,随后导致膜的通透性增加。如负染色电子显微镜所示,用 PCI 处理大肠杆菌或化脓性链球菌会引发膜破裂,随后细菌细胞质内容物外溢和细菌杀伤。PCI 的抗菌活性位于该蛋白的肝素结合位点,跨越该区域的肽被发现模拟 PCI 的抗菌活性,而不会导致真核细胞的裂解或膜破坏。最后,我们表明,血小板在激活时可以在其表面组装 PCI。由于血小板被募集到细菌感染部位,这些结果可以解释我们的发现,即患有由化脓性链球菌引起的坏死性筋膜炎的患者的组织活检中 PCI 水平升高。总之,我们的数据描述了 PCI 在先天免疫中的一个新功能。